Abstract: A device useful for accessing the left atrium is provided. The device comprises an elongated tubular body and a dilating tip. The tubular body has an axis, a proximal end, a distal end and a lumen longitudinally extending therethrough. The dilating tip is slidably mounted on the distal end of the tubular body. The dilating tip comprises a segmented surface that is generally transverse to the axis of the tubular body, and a generally rigid tube extending distally from the segmented surface and having a sharp distal end. Distal movement of the tubular body relative to the dilating tip exerts a force on the segmented surface to thereby open the segmented surface.

Abstract: Embodiments are described for creating and closing tissue access ports, such as transapical access ports, which involve placement of an introducer across the subject tissue structure, and deployment of a controllable port closure device assembly configured to remain in place with a ratcheting mechanism, and to hold the tissue surrounding the previous access port location closed against a sealing disc with proximal and distal strut assemblies, after the introducer has been removed.

Abstract: A device, system and method for orthopedic spine surgery using a novel screw-based retractor, disclosed herein, that allows for access to the spine through a minimally or less invasive approach. The retractor device is designed to be coupled to a pedicle screw and then to have opposed arms of the retractor spread apart to open the wound proximally. The retractor is removed by pulling it out of the wound whereby the retractor is deformed to pass over the pedicle screw head. The retractor is intended to be made of a stiff plastic material, sterile packaged and disposable after one use. A system and method for using the retractor and performing a minimally invasive spine surgical procedure are also disclosed.

Abstract: A pedicle screw and rod assembly that has particular application for minimally invasive percutaneous pedicle screw instrumentation. The assembly includes pedicle screws having ball-shaped heads that are threaded through pedicles of adjacent vertebra into the vertebral body. The assembly also includes two cannulated posts that extend above a cannulated pedicle screw to allow placement over a K-wire. A head portion accepts the head of the pedicle screw in a secure and multi-axial engagement. The assembly further includes a tube portion that is coupled to the head portion and extends above the patient's skin. The assembly also includes a lordotic slotted rod that is slid down the tube portions to be positioned on top of the head portions of the posts so that the portions are locked within the slot. Bolts are then slid down the tube portions and are threaded to a threaded portion on the portion.

Abstract: A bone anchor assembly includes a bone anchor having a proximal head and a distal shaft configured to engage bone, a receiver member for receiving a spinal fixation element to be coupled to the bone anchor, an insert positioned in the proximal end of the receiver member having a pair of spaced apart insert arms defining a recess therebetween, and a closure mechanism positionable between and engaging the insert arms to capture a spinal fixation element within the recess of the insert and fix the spinal fixation element with respect to the receiver member.

Abstract: An implantable spacer for placement between adjacent spinous processes in a spinal motion segment is provided. The spacer includes a body defining a longitudinal axis and passageway. A first arm and a second arm are connected to the body. Each arm has a pair of extensions and a saddle defining a U-shaped configuration for seating a spinous process therein. Each arm has a proximal earning surface and is capable of rotation with respect to the body. An actuator assembly is disposed inside the passageway and connected to the body. When advanced, a threaded shaft of the actuator assembly contacts the earning surfaces of arms to rotate them from an undeployed configuration to a deployed configuration. In the deployed configuration, the distracted adjacent spinous processes are seated in the U-shaped portion of the arms.

Abstract: An orthopaedic device to realign bone segments comprises first and second attachment members and a strut or spacer member. The first attachment member is attached to a first rib bone or first transverse process or first lamina of a vertebra. The second attachment member is attached to a second rib bone or second transverse process or second lamina of a vertebra. The strut is positioned between the first and second attachment members. The strut is fixedly or releasably connected to the first and second attachment members to couple the first attachment member to the second attachment member. The strut provides distraction between the first and second rib bones or transverse processes to realign the rib bones. The attachment members comprise a clamp and screw combination.

Abstract: Methods and apparatus provide for coupling an elongate guide substantially at a first end to at least one vertebral body of a spinal column of a patient; and extending a second end of the guide to a structure of the patient spaced in an anterior direction away from the at least one vertebral body towards an entry incision.

Abstract: Minimally invasive methods and devices for introducing a spinal fixation element into a surgical site in a patient's spinal column are provided. In general, the method involves advancing a spinal fixation element in a first, lengthwise orientation along a pathway extending from a minimally invasive percutaneous incision to a spinal anchor site. As the spinal fixation element approaches the spinal anchor site, the fixation element can be manipulated to extend in a second orientation, which is preferably substantially transverse to the first orientation, to position the fixation element in relation to one or more spinal anchors.

Abstract: Featured is a reduction instrument being configured and arranged to allow correction of vertebral translation and applying distraction across a segment in an independent fashion. Such a reduction instrument embodies one or more identical modules that are configured as needed for correcting the deformity. In more particular embodiments, each of the one or more modules has two degrees of freedom (DOF) with uncoupled orthogonal translations. Such a reduction instrument allows the reorientation of the vertebral segment as needed via uncoupled orthogonal translations. Such a reduction instrument also is usable in combination with a plurality of vertebral anchors, such vertebral anchors being any such vertebral anchors as are know to those skilled in the art (e.g., conventional spinal pedicle screw instrumentation) or hereinafter developed so as to form a spinal implant system. Also featured are treatment methods utilizing such a reduction instrument.

Abstract: Spinal rod reduction apparatuses, systems, and methods are provided. In various examples, a rod reduction apparatus includes a first threaded member (130, 210, 330) including an engagement feature (138A, 138B, 220, 332, 334) configured to selectively anchor the first threaded member to the implantable screw assembly. A second threaded member (110, 230, 310) is configured to threadably engage with the first threaded member. The second threaded member is axially movable with respect to the first threaded member with rotation of the second threaded member. A spinal rod urging member (120, 240, 320) is axially movable with the second threaded member. The urging member includes a bearing surface (126, 242, 320) that is configured to selectively abut the spinal rod and selectively urge the spinal rod toward the implantable screw assembly with rotation of the second threaded member in a first rotational direction.

Abstract: A method for fusing a joint, which includes the step of inserting a first anchoring zone of an arthrodesis device being in a first closed position into a first opening within a first bone. The first anchoring zone includes a first pair of legs. Each leg is capable of transitioning between the first closed position and a first open position for internally gripping the first opening. Also, included in the method is the step of inserting a second anchoring zone of the arthrodesis device being in a second closed position into a second opening within a second bone. The second anchoring zone includes a second pair of legs. Each leg is capable of transitioning between the second closed position and a second open position for internally gripping the second opening.

Abstract: An adjustable length orthopedic device and system. According to one embodiment, the adjustable length orthopedic device or system comprises an elongated shaft with a longitudinal axis, and an adjustable portion extending from a proximal end of the elongated shaft along the longitudinal axis. The adjustable length orthopedic device further comprises at least one hole in a distal end portion of the device, where the hole is adapted for insertion of a pin through the device and into the bone in order to anchor the device to the bone. According to another embodiment is a lag screw extending from a proximal end of the elongated shaft at an angle oblique to the longitudinal axis, the lag screw comprising a lag screw shaft segment, and an adjustable segment that extends from the proximal end of the shaft segment. According to another embodiment is an adjustable length locking screw.

Abstract: A bone plate includes an upper surface, a bone contacting surface, and at least one hole extending through the upper and bone contacting surfaces for receiving a bone screw. The at least one hole includes a first portion and a second portion that overlap one another. The first portion defines a substantially circular outer periphery and the second portion defines an elongated outer periphery that is elongated in a direction substantially parallel to the longitudinal axis of the plate. The first portion may have threads configured to engage threads on the head of a bone screw, and the second portion may be configured to cooperate with the head of a different bone screw to provide compression to the fracture.

Abstract: A surgical assembly has a first section having a first hole with a smallest diameter and a second section having a threaded second hole with a minor thread diameter smaller than the smallest diameter of the first hole. The first hole encloses a center axis of the second hole and a clearance is provided between the first section and the second section. The assembly includes a screw member having a length for engaging the first hole and the second hole so as to bridge the clearance. The screw member has a first portion with a largest outer diameter smaller than or equal to the smallest diameter of the first hole, and a threaded second portion axially spaced from the first portion and configured to threadedly engage the second hole. A major thread diameter of the second portion is larger than the smallest diameter of the first hole.

Abstract: A method of repairing bone. In the method, a sleeve and a fastener may be provided, with the fastener projecting from the sleeve and having a trailing section disposed in threaded engagement with the sleeve. A leading section of the fastener may be driven into threaded engagement with bone. The sleeve may be advanced into contact with the bone to apply tension to the fastener and compress the bone. A trailing section of the fastener may be driven out of the sleeve and into threaded engagement with the bone.

Abstract: An anchor for a pedicle screw having an anchor body comprising a proximal end, a proximal portion, a distal portion, and a distal end, and a through-hole through the anchor body from the proximal end to the distal end. The through-hole defines a long axis of the anchor, and is provided with undersized female threads in the proximal portion and a reduced inner diameter in the distal portion. The reduced inner diameter causes expansion of at least the distal portion of the anchor body when a screw is inserted into the through-hole. The anchor is further provided with a plurality of ridges on an exterior surface of the anchor body, the ridges configured to reduce the likelihood of pullout when the anchor is inserted into a vertebra and a screw is inserted into the through-hole.

Abstract: A bone plate system for osteosynthesis comprises a bone plate, a swivel screw, a clamping screw, a swivel hole formed in the bone plate as a through hole for receiving the swivel screw polyaxially, and a clamping hole, which is associated with the swivel hole and is formed in the bone plate as a further through hole for receiving the clamping screw. When the swivel screw and the clamping screw are screwed in, they are fixed with angular stability in multiple dimensions, as the screw heads of the swivel screw and of the clamping screw are secured by one another and by the bone plate against relative movement. The swivel screw and the clamping screw are each designed as a bone screw.

Abstract: The present invention is directed to devices and methods that can be used in ankle surgery, especially ankle fusion surgery.

Abstract: Systems and methods for treating bone, such as vertebral compression fractures are disclosed. A method includes controllably applying energy to a bone cement volume outside of a patient's body to selectively accelerate the polymerization rate of the bone fill material volume prior to introduction into a bone. The method further includes sequentially introducing a plurality of cement carrying structures with the accelerated polymerization rate bone cement volume into the bone. A system for use in the method includes at least one elongated cement-carrying structure sized to carry a bone cement volume therein and an energy source operatively coupleable to the cement-carrying structure. The energy source applies energy to the bone cement volume to selectively accelerate a polymerization rate thereof. An elongated injector insertable into the bone has a passageway that removably receives the elongated cement-carrying structure to allow delivery of the accelerated polymerization rate bone cement into the bone.

Abstract: Systems and methods for treating vertebral compression fractures are provided. A kit can include at least one body containing a bone cement precursor to be mixed with at least one other bone cement precursor to form a bone cement. The body or a package containing the body can include at least one sensor. In some embodiments the sensor can be a temperature sensor. In some methods, data from the sensor can be used to determine certain parameters related to a treatment interval involving the bone cement.

Abstract: A surgical instrument comprises a first member including an inner surface that defines a cavity and an outer surface configured to space tissue. The first member includes a first locking surface. A second member is configured for disposal within the cavity and extends between a first end configured to penetrate tissue and a second end configured to generate a signal representative of a position of the second member. The second member includes a second locking surface. The members are disposable between a first orientation such that the locking surfaces are engaged to resist relative axial translation of the members and a second orientation such that the locking surfaces are disengaged and the second member is axially translatable relative to the first member. Systems and methods are disclosed.

Abstract: A device for treating fractures of a bone comprises a plurality of arms, each extending from a proximal end to a distal end and movable in a three-dimensional space, the proximal end of each arm coupled to a frame and a plurality of couplings, each of the couplings coupled to a distal end of each of the plurality of arms, the coupling lockingly receiving a bone fixation element secured to a corresponding bone fragment such that each of the arms is coupled to a corresponding fragment of the bone in combination with a mechanical unit moving each of the arms relative to the frame and a controller receiving data corresponding to a desired final position of the fragments relative to one another and controlling the mechanical unit to move the arms relative to one another to achieve the desired final position of the bone fragments relative to one another.

Abstract: A system and method for tissue thermotherapy including a source for generating a vapor phase media for treating a space in a human body, such as and intraluminal or intracavity space. The system further includes a filtering member for allowing a recirculation of flowable media about an interface with tissue, wherein the filtering member prevent ablation detritus from interfering with media outflows from the working end.

Abstract: Methods, apparatus, and systems for treating tissue located beneath a tissue surface with electromagnetic energy delivered from a treatment electrode. The treatment electrode may include a conductive layer and a plurality of openings extending through the conductive layer. The openings may vary in size or area across the conductive layer, and may vary progressively in size or area with location relative to the electrode perimeter.

Abstract: An electrosurgical device comprises an end effector, a cutting member, and en electromechanical driver. The end effector comprises a pair of jaws that clamp tissue. The jaws include electrodes that deliver RF energy to clamped tissue. The cutting member cuts tissue clamped between the jaws. The electromechanical driver drives the cutting member. A control module commands the electromechanical driver, and regulates the delivery of RF energy to the electrodes, based on a combination of user input and feedback signals from the electrodes and from the electromechanical driver. The device may provide tactile feedback to the user through the user input feature, based on a load encountered by the cutting member. The device may alert the user when the exterior of end effector makes incidental contact with tissue, to avoid inadvertently burning the tissue. The device may include a removable battery pack to power the electromechanical driver and the electrodes.

Abstract: This treatment instrument (1) for an endoscope is provided with a treatment section (2) for treatment, an operation wire (2) connected with the treatment section (2), a coil sheath (9) into which the operation wire (3) is inserted, an insulating tube (10) into which the coil sheath (9) is inserted, and an operation section (4) for operating the treatment section (2). The operation section (4) comprises a slider (15) rotatably connected with the operation wire (3), a body (13) to which the slider (15) is mounted movably forward and backward, and a rotational operation section (14) which is so mounted as to be rotatable with respect to the body (13) and has the coil sheath (9) so mounted thereto as to be not rotatable. The distal end of the insulating tube (10) is mounted rotatably and movably forward and backward to the distal end of the coil sheath (9).

Abstract: An instrument for use in a medical procedure that includes a proximal end, a distal end, a handle adjacent to the proximal end of the instrument, a flexible elongated neck extending distally from a distal end of the handle, a jaw power screw extending from a distal end of the neck, a pair of moveable jaws operatively connected to the jaw power screw, and a handle power screw assembly operatively connected to a proximal end of the flexible neck within the handle, wherein manipulation of the handle will control movement of the jaws.

Abstract: An electrosurgical vessel sealing instrument having a first and a second opposing jaw member at a distal end thereof, wherein each jaw member includes a jaw housing, a seal plate having a tissue contacting surface and a side wall, and an insulating region disposed on the side wall of the seal plate. The instrument includes the ability to move the jaw members relative to one another from a first position wherein the jaw members are disposed in spaced relation relative to one another to a second position wherein the jaw members cooperate to grasp tissue. The insulating region enables precision overmolding of the jaw housing to the seal plate, while advantageously reducing thermal spread and edge cutting during vessel sealing procedures.

Abstract: An endoscopic forceps is provided and includes a housing having a shaft that extends therefrom. An end effector assembly is operatively connected to a distal end of the shaft and includes a pair of pivotably coupled first and second jaw members. The jaw members are movable relative to one another. A drive mechanism includes a driving structure. A link assembly includes two or more links that are operably coupled to each other and the drive structure. The two or more links are operably coupled to respective ones of the first and second jaw members.

Abstract: An apparatus for endobronchial ablation of a tumor is provided. The apparatus has an ablation catheter and a guide facility to be inserted into the bronchial system, a sheath defining a guide channel for the ablation catheter, a closing apparatus for a bronchial arm, and an aperture allowing airtight insertion of the ablation catheter into a bronchial arm blocked by the closing apparatus. The ablation catheter and/or the guide facility have a suction apparatus for sucking air out of a bronchial arm blocked off by the closing apparatus.

Abstract: Methods and devices that displace bone or other hard tissue to create a cavity in the tissue. Where such methods and devices rely on a driving mechanism for providing moving of the device to form a profile that improves displacement of the tissue. These methods and devices also allow for creating a path or cavity in bone for insertion of bone cement or other filler to treat a fracture or other condition in the bone. The features relating to the methods and devices described herein can be applied in any region of bone or hard tissue where the tissue or bone is displaced to define a bore or cavity instead of being extracted from the body such as during a drilling or ablation procedure.

Abstract: Apparatuses, compositions and methods for removing cells which interfere with regenerative processes. The apparatuses, compositions and methods selectively kill partially functional and/or non-functional cells versus functional cells while protecting functional proliferative cells to the extent that, upon removal of the killed cells by disintegration or scavenging, functional cells replace the partially- or non-functional cells.

Abstract: A radiation applicator with a dielectric body (2) surrounding the antenna. The dielectric body (2) is comprised of three sections (3, 4 and 5) with different dielectric constants to provide broad-band matching of the applicator to surrounding material. Washers (10) and (11) are mounted on the antenna to act as reflectors.

Abstract: A surgical device is disclosed, and includes a pair of finger-mountable annular members, each having an electrode disposed thereon. An optical member is disposed on at least one of the pair of finger-mountable annular members and has a first set of light transmitting properties corresponding to a first set of physical parameters of at least one of the finger-mountable annular members. At least one finger-mountable annular member is configured to transition to a second set of physical parameters being different from the first set of physical parameters. The optical member is configured to transition from a first set of light transmitting properties to a second set of light transmitting properties, the second set of light transmitting properties corresponding to the second set of physical parameters, the second set of light transmitting properties being different from the first set of light transmitting properties.

Abstract: A RF energy console controls RF energy output from a RF generator for sealing blood vessels. The energy console includes a processor that executes routines and a controller feedback circuit that, in combination, control the RF generator. Operation includes a heating stage outputting a RF ramping voltage and determining a decrease in measured current to less than a predetermined % percentage of a maximum measured and stored current value to advance to a sealing stage. Then, the voltage is controlled to maintain an increasing change in impedance until a change in current value approaches a flat curve indicating seal completion, which stops the RF generator output. To reseal or enhance a blood vessel seal, the energy console executes the same routines as in the initial sealing operation.

Abstract: A method of manufacturing a microwave ablation device, the method including applying a balun short circumferentially about an outer conductor of a coaxial feedline and applying a dielectric material circumferentially about the outer conductor of the coaxial feedline and in contact with the balun short to form a balun. The method further including extending a temperature sensor along the coaxial feedline such that the sensor contacts the balun short, securing the temperature sensor to the coaxial feedline with a first heat shrink material, and securing the dielectric material, balun short, and temperature sensor in contact with each other and to the coaxial feedline using a second heat shrink material.

Abstract: A dermatological laser apparatus for irradiating human tissue with optical pulses includes a laser source (2) producing an optical output, a pulse shaper (4) coupled to the laser source for converting the optical output into optical pulses having desired shapes, and an optical delivery tool (8) coupled to the pulse shaper for applying the optical pulses sequentially to a multiplicity of sites on the human tissue with consecutively irradiated sites being non-adjacent.

Abstract: A fluoroscopy C-arm drape clip for attaching a sterile drape to a C-arm of a fluoroscopy C-arm imaging unit and method of providing a sterile outer surface on a C-arm of a fluoroscopy C-arm imaging unit is provided. The drape clip includes a generally U-shaped band having a pair of legs and an arm. Each of the legs has a first end attached to the arm and a second end spaced from the arm. The legs extend away from the arm in non-parallel, laterally spaced relation with one another and have inner surfaces facing one another and an outer surfaces facing away from one another. Further, an elastic pad is attached to the inner surface of each of the legs adjacent the second ends.

Abstract: A robotic system for manipulating a catheter with a plurality of steering wires longitudinally situated within a length of the catheter includes a user interface configured to display a view of an anatomical model and to receive one or more user inputs; a catheter manipulator assembly configured to linearly actuate one or more control members of a catheter; and a robotic controller configured to provide a view of an anatomical model to the user interface; accept one or more user inputs from the user interface; register the one or more user inputs to a coordinate system associated with the anatomical model; compute one or more actuator commands from the one or more registered inputs; and cause the catheter manipulator assembly to linearly actuate one or more control members of a catheter in accordance with the computed actuator commands.

Abstract: A device for holding a surgical tool includes a first member extending along a longitudinal axis between a first end and a second end. The first end includes an inner surface defining a conduit extending transverse to the longitudinal axis. The conduit includes a first portion and a second portion defining a first chamber. A cap has an inner surface including a first section configured to engage an outer surface of the first member and a second section defining a second chamber extending transverse to the longitudinal axis. The second chamber is in communication with the first chamber when the cap engages the first member such that the first and second chambers define a cavity. A pivoting member is movably disposed in the cavity and includes an inner surface defining a passageway. A second member is disposed within the passageway. Methods of use are disclosed.

Abstract: An adjustable support apparatus used to support a person in a specific position over an extended period of time, and method of using the same. The apparatus has a base, an adjustable plate clamp assembly with upper and lower plates, a pivot within the apertures of the plates and adjustably retained between the plates, and a support member attached to the pivot and adapted to support a load. The adjustable plate clamp assembly has upper and lower plates. The upper plate has a central upper aperture, a first end pivotally attached to the base, and a second end. The lower plate has a central lower aperture, a first end, and a second end pivotally attached to the second end of the upper plate. The first end of the lower plate bears against the base, the plates together form an acute angle, and the apertures are aligned with one another.

Abstract: An illuminating ring assembly is disclosed. The illuminating ring configured to be used with a surgical access element. The illuminating ring assembly comprises a housing defined by a cover and a wall member extending from the cover, wherein the cover and wall member cooperate to define a cavity therein, a light element configured to be disposed with the cavity, and an attachment mechanism configured to selectively attach the housing to a surgical access element. Wherein the cover and the light element both include an opening therethrough.

Abstract: A method for replacing a portion of a target bone in a living body includes the steps of attaching one or more first markers to a target bone, establishing a medical three-dimensional representation of the target bone, performing a virtual resection of a resection portion, the virtual resection constructing a three-dimensional representation of the resection portion and a three-dimensional representation of the remaining target bone including cutting edges, providing a virtual pattern of the resection portion, obtaining an implant or graft portion for replacing the resection portion of the target bone by using the virtual pattern of the resection portion, resecting the resection portion from the target bone according to the virtual resection using the first reference system of coordinates and coupling the implant or graft portion to the target bone in a position substantially matching a position of the resection portion before the actual resection.

Abstract: Among various methods, systems, and apparatuses, a number of methods are provided for forming a 3D conformance model of a particular portion of a subject's anatomy using 3D digitized imaging data and a rapid prototyping technique. One such a method includes distinguishing at least one particular structural feature associated with the exterior of the particular portion from at least one particular structural feature associated with the interior of the particular portion. Such a method can include using the conformance model to test suitability of an appliance to participate in performing an intended function that includes penetrating the interior of the particular portion through the exterior of the particular portion.

Abstract: Orthodontic systems and related methods are disclosed for designing and providing improved or more effective tooth moving systems for eliciting a desired tooth movement and/or repositioning teeth into a desired arrangement. Methods and orthodontic systems of the invention include tooth attachments having improved or optimized parameters selected or modified for more optimal and/or effective application of forces for a desired/selected orthodontic movement. Attachments of the present invention can be customized to a particular patient (e.g., patient-customized), a particular movement, and/or a sub-group or sub-set of patients, and configured to engage an orthodontic tooth positioning appliance worn by a patient, where engagement between the attachment and orthodontic appliance results in application of a repositioning force or series/system of forces to the tooth having the attachment and will generally elicit a tooth movement.

Abstract: A computer is used to create a plan for repositioning an orthodontic patient's teeth. The computer receives an initial digital data set representing the patient's teeth at their initial positions and a final digital data set representing the teeth at their final positions. The computer then uses the data sets to generate treatment paths along which the teeth will move from the initial positions to the final positions.

Abstract: A coupling assembly, particularly for dental implants, having at least one pin, which can be coupled rigidly to a bone portion, and a supporting element, which can be associated with a prosthesis. The pin has, at its end portion that lies opposite the one designed for connection to the bone portion, a protruding tab that can be accommodated by elastic forcing in a respective cavity formed in the supporting element so as to produce a stable coupling configuration between the pin and the supporting element. The tab is shaped like a substantially equatorial portion of a sphere with an outer lateral surface adapted to abut, with at least one part thereof, against the internal side wall of the cavity, to determine stable coupling configuration.

Abstract: For producing a mother matrix mould of a full or partial dental prosthesis or of a temporary crown or bridge or of a permanent crown or bridge, the data of a digitalised virtual model reflecting the status of the jaw is used to generate a data set of the digital tooth set-up of the full or partial dental prosthesis or of the temporary crown or bridge or of the permanent crown or bridge, based on which a rapid manufacturing or rapid prototyping method is used to produce a functional model of the full or partial dental prosthesis or of the temporary crown or bridge or of the permanent crown or bridge that is then invested in a curable elastic impression material from which the mother matrix mould is produced after curing the elastic impression material.

Abstract: A prophy angle is provided that includes a paste-dispensing assembly that includes an actuator at the proximal end of the housing, and a push rod linked to the actuator and supporting a plunger on the push rod, where the push rod is supported by the housing in a biased manner to permit longitudinal movement within the housing in a reciprocating manner as actuated by the actuator, to dispense a controlled quantity of paste out of the prophy angle.